Related gene-specific medical variations for Gene (Select 56985) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1272930	NM_020233.5(ADPRM):c.-18+76G>C	ADPRM, LOC112529895 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258787	NM_020233.5(ADPRM):c.-18+149_-18+150insG	ADPRM, LOC112529895 +1 more	Insertion (intron variant)	not provided	GBenign
Select item 1240455	NM_020233.5(ADPRM):c.-31G>A	ADPRM, LOC112529895 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1237522	NM_020233.5(ADPRM):c.-87G>A	ADPRM, LOC112529895 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1223633	NM_020233.5(ADPRM):c.-18+136C>T	ADPRM, LOC112529895 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1213105	NM_020233.5(ADPRM):c.-18+52T>G	ADPRM, LOC112529895 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar